Certara is a leading company dedicated to accelerating the development of impactful medicines that improve society and the lives of those who need them most. With a dynamic work environment that fosters innovation and creativity, Certara offers opportunities for continuous training and development. The company’s extensive portfolio covers all phases of drug development, collaborating with over 1,200 commercial companies, 250 academic institutions, and various regulatory agencies.
Job Overview
The Data Analyst Level 2 position involves interpreting clinical trial data across various therapeutic areas and contributing to the development of database products that facilitate informed decision-making throughout the clinical development and post-approval phases. Candidates should have a strong background in pharmacology and clinical research, along with experience in developing clinical databases for systematic literature reviews and meta-analyses.
Responsibilities
As a Data Analyst Level 2, you will be responsible for:
- Clinical Database Development: Play a crucial role in creating high-quality clinical database products across various therapeutic areas, including Metabolic & CV, Neuroscience, Autoimmune, Oncology, and Respiratory, supporting different types of meta-analyses (pairwise, network, and model-based).
- Data Analysis and Annotation: Analyze and annotate trial design, treatment information, demographics, and outcome data (biomarkers, clinical, safety, and quality of life) derived from clinical literature such as journals, conference abstracts, and regulatory reviews.
- Digitization of Results: Accurately digitize results from graphical representations of outcomes reported on linear, logarithmic, and semi-log scales.
- Collaboration and Quality Assurance: Work closely with the lead consultant, peer data analysts, and quality manager to understand and enhance database rules, specifications, and quality processes.
- Continuous Learning: Participate in training programs related to statistics, R coding, systematic literature review, and data analysis methods to develop your skills and advance in the organization.
Qualifications
To be eligible for this role, candidates should have:
- A Master’s degree in Pharmacology, Pharmaceutics, Clinical Practice, Public Health, or Epidemiology, preferably with relevant experience.
- A minimum of 1-2 years of experience in information science, systematic literature review, health economics, or public health sectors; pharmaceutical industry experience is preferred.
- Strong knowledge of pharmacology and clinical research.
- Familiarity with clinical development phases, the PICOS approach, trial designs, and industry data standards/ontologies.
- Knowledge of statistics and data management tools, such as R, is a plus.
- Excellent interpersonal and communication skills, with a collaborative mindset.
